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Synthesis and Some Reactions of 1-α-Cyanoalkyl(aralkyl)-2-pyrazolines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

1-α-Cyanoalkyl(aralkyl)-2-pyrazolines were obtained by the reaction of 1-alkylidene(arylidene)-2-pyrazolinium tetrafluoroborates with metal cyanides. Reduction of the products led to substituted β-aminoalkyl-2-pyrazolines. Hydrolysis of the nitrile groups gave the corresponding substituted acetamides.

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Authors and Affiliations

  1. Chemistry Faculty, M. V. Lomonosov Moscow State University, Moscow, 199899, Russia

    N. I. Vorozhtov & G. A. Golubeva

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  1. N. I. Vorozhtov
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  2. G. A. Golubeva
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, 10, 1558–1565, October 2005.

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Vorozhtov, N.I., Golubeva, G.A. Synthesis and Some Reactions of 1-α-Cyanoalkyl(aralkyl)-2-pyrazolines. Chem Heterocycl Compd 41, 1307–1313 (2005). https://doi.org/10.1007/s10593-005-0317-y

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